Canonical Allele Identifier: PA2830264972
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2496514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu576Gly
CA398529773
NM_144997.7:c.1727A>G